Pharmacology of adenosine A2A receptors and therapeutic applications

被引:104
作者
Fredholm, BB
Cunha, RA
Svenningsson, P
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
[2] Univ Coimbra, Inst Biochem, Ctr Neurosci, Coimbra, Portugal
[3] Rockefeller Univ, New York, NY 10021 USA
关键词
methylxanthines; purines; basal ganglia; inflammation; knock-out;
D O I
10.2174/1568026033392200
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Adenosine A(2A) receptors were cloned about ten years ago and are known to be well conserved among mammals. Rather selective agonists and antagonists are available. In addition, two different knock-out mice have been prepared and extensively characterized. A(2A) receptors are highly enriched in the basal ganglia and on cells involved in inflammatory reactions. At these sites they are likely to play physiologically important roles. Efforts to develop new therapies based on A(2A) receptors have focused on these topics. However, A(2A) receptors are found on many other cell types and on them as well agonists can exert effect.
引用
收藏
页码:413 / 426
页数:14
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